A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156413



Internal ID22086814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177730398..177771448hg38UCSC Ensembl
Outerchr5:177724103..177800550hg38UCSC Ensembl
Innerchr5:177157399..177198449hg19UCSC Ensembl
Outerchr5:177151104..177227551hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3876448
hg1976448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016797, nssv4016821, nssv4016808, nssv4016809, nssv4016828, nssv4016798, nssv4016822, nssv4016733, nssv4016792, nssv4016800, nssv4016778, nssv4016730, nssv4016787, nssv4016762, nssv4016784, nssv4016766, nssv4016819, nssv4016802, nssv4016801, nssv4016729, nssv4016740, nssv4016830, nssv4016810, nssv4016785, nssv4016754, nssv4016727, nssv4016813, nssv4016781, nssv4016814, nssv4016833, nssv4016755, nssv4016805, nssv4016775, nssv4016744, nssv4016764, nssv4016804, nssv4016739, nssv4016774, nssv4016728, nssv4016753, nssv4016771, nssv4016759, nssv4016786, nssv4016746, nssv4016777, nssv4016829, nssv4016767, nssv4016734, nssv4016793, nssv4016823, nssv4016732, nssv4016803, nssv4016815, nssv4016770, nssv4016756, nssv4016820, nssv4016788, nssv4016794, nssv4016827, nssv4016824, nssv4016743, nssv4016751, nssv4016795, nssv4016772, nssv4016832, nssv4016735, nssv4016782, nssv4016760, nssv4016769, nssv4016747, nssv4016783, nssv4016745, nssv4016750, nssv4016818, nssv4016817, nssv4016768, nssv4016737, nssv4016791, nssv4016748, nssv4016731, nssv4016807, nssv4016796, nssv4016789, nssv4016825, nssv4016765, nssv4016811, nssv4016780, nssv4016812, nssv4016779, nssv4016799, nssv4016763, nssv4016790, nssv4016757, nssv4016736, nssv4016742, nssv4016806, nssv4016826, nssv4016738, nssv4016758, nssv4016761, nssv4016831, nssv4016816, nssv4016752, nssv4016741, nssv4016776, nssv4016749, nssv4016773
Samples
Known GenesFAM153A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156413
Frequency
Sample Size131
Observed Gain0
Observed Loss107
Observed Complex0
Frequencyn/a


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